FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862052964 · Model: 207-10-09 · Exactech, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862052964
Version / Model
207-10-09
Catalog Number
207-10-09
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-28
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
eca27663-5c2a-4ae0-b5b0-e00c76f8a7df

Device Description

DISTAL RESECTION ASSESSMENT DEVICE, FAAD

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10885862052964

Premarket Submissions

Submission Number Supplement Number
K011976 000
K032606 000
K033883 000
K932690 000
K932776 000
K933494 000
K933610 000